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| created at |
2024-09-23 16:23:50 UTC |
| updated at |
2024-09-23 18:22:39 UTC |
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Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
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20,514 entries
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There is 0 pattern entry.
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Peeling skin syndrome 2
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Orphanet_263534 |
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Peeling skin syndrome type A
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Orphanet_263548 |
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Peeling skin syndrome type B
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Orphanet_263553 |
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Poorly differentiated thymic neuroendocrine carcinoma
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Orphanet_263339 |
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Hyperinsulinism due to INSR deficiency
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Orphanet_263458 |
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SDCD, CHST3 type
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Orphanet_263463 |
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SEMD, Maroteaux type
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Orphanet_263482 |
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Pseudo-Morquio syndrome type 2
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Orphanet_263482 |
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CDG syndrome type IIg
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Orphanet_263508 |
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CDG syndrome type IIi
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Orphanet_263487 |
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CDG syndrome type IIj
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Orphanet_263501 |
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CDG syndrome type Io
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Orphanet_263494 |
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Postcardiotomy right ventricular failure
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Orphanet_263352 |
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